8 results
·
36ms
·
Sources: EU EUDAMED, US FDA
PEDIATRIC VEST RESTRAINT
FDA 510(k)
FDA Class 1
·General Hospital
Intra.Ox Handheld Tissue Oximeter
FDA 510(k)
FDA Class 2
·Cardiovascular
ULTRASONIC BIOMETER/ PACHYMETER FOR OPHTHALMOLOGY, MODEL ODM 2100, 2200
FDA 510(k)
FDA Class 2
·Radiology
GYNECARE X-TRACT MORCELLATOR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code HET·June 16, 2006
SCREW,FIXATION,BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·July 11, 2016
SNAP-OFF SCREW 2.7MM LENGTH 14MM
FDA Adverse Event
Malfunction
·NEWDEAL SAS·Product code HWC·May 30, 2014
PERQCATH CATHETER
FDA Adverse Event
Malfunction
·C. R. BARD INC. (BASD)·Product code LJS·December 20, 2010
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·February 15, 2013